Reacción #996528
ord-fe06b0af90f045d88051afe5b3b469fd
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1OtroThe vial was flushed with nitrogen
- 2Otrosealed with a Teflon-
- 3Otrolined cap
- 4Otroplaced in an oil bath
- 5TemperaturaThe reaction was cooled to ambient temperature
- 6workup.ADDITIONdiluted with chloroform
- 7Filtraciónfiltered through a bed of CELITE
- 8Filtraciónfilter agent
- 9OtroThe solvent was evaporated
- 10Otrothe residue was purified by column chromatography on a Biotage Horizon™ High-Performance Flash Chromatography instrument
- 11OtroThe purification
- 12Lavadowas carried out eluting with chloroform
- 13OtroAdditional purification
- 14Otroby recrystallization from acetonitrile
Procedimiento
7-Bromo-2-ethoxymethyl-1-(3-isopropoxypropyl)-1H-imidazo[4,5-c]quinolin-4-amine (0.75 g), 2(1H)-pyridone (0.20 g), copper(I) iodide (68 mg), N,N′-dimethylethylenediamine (75 μL), potassium phosphate (0.79 g) and dioxane (2.7 mL) were added to a scintillation vial. The vial was flushed with nitrogen, sealed with a Teflon-lined cap, placed in an oil bath, and heated to 110° C. for 60 hours. The reaction was cooled to ambient temperature, diluted with chloroform and filtered through a bed of CELITE filter agent. The solvent was evaporated and the residue was purified by column chromatography on a Biotage Horizon™ High-Performance Flash Chromatography instrument using a silica gel cartridge. The purification was carried out eluting with chloroform:CMA in a gradient from 99:1 to 75:25. Additional purification by recrystallization from acetonitrile provided 0.38 g of 1-[4-amino-2-ethoxymethyl-1-(3-isopropoxypropyl)-1H-imidazo[4,5-c]quinolin-7-yl]-1H-pyridin-2-one as a tan solid, mp 161-163.5° C.